Evidence map›Paper›PMID 27681508›Full record

ArticlePloS one

Alternative Splice Variants Modulates Dominant-Negative Function of Helios in T-Cell Leukemia.

Shaorong Zhao, Wei Liu, Yinghui Li, Pengjiang Liu, Shufang Li, Daolei Dou, Yue Wang, Rongcun Yang, Rong Xiang, Feifei Liu

Open access · goldAbstract read
In one paragraph

Article in PloS one. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.7field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 4 institutions in 1 country.

Shaorong ZhaoDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Wei LiuTianjin Entry-Exit Inspection and Quarantine Bureau, Tianjin 300308, China.
Yinghui LiDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Pengjiang LiuDepartment of Hematology, First-Central Hospital, Tianjin 300060, China.
Shufang LiDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Daolei DouState Key Laboratory of Medical Chemical Biology, Tianjin 300070, China.
Yue WangDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Rongcun YangDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Rong XiangDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Feifei LiuDepartment of Immunology, School of Medicine, Nankai University, Tianjin 300071, China.
Nankai University · CNEntry Exit Inspection and Quarantine Bureau · CNState Key Laboratory of Medicinal Chemical BiologyTianjin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The molecular defects which lead to multistep incidences of human T-cell leukemia have yet to be identified. The DNA-binding protein Helios (known as IKZF2), a member of the Ikaros family of Krüppel-like zinc-finger proteins, functions pivotally in T-cell differentiation and activation. In this study, we identify three novel short Helios splice variants which are T-cell leukemic specific, and demonstrate their dominant-negative function. We then test the cellular localization of distinct Helios isoforms, as well as their capability to form heterodimer with Ikaros, and the association with complexes comprising histone deacetylase (HDAC). In addition, the ectopic expression of T-cell leukemic Helios isoforms interferes with T-cell proliferation and apoptosis. The gene expression profiling and pathway analysis indicated the enrichment of signaling pathways essential for gene expression, translation, cell cycle checkpoint, and response to DNA damage stimulus. These data indicate the molecular function of Helios to be involved in the leukemogenesis and phenotype of T-cell leukemia, and also reveal Helios deregulation as a novel marker for T-cell leukemia.

Identifiers

PMID27681508
PMCPMC5040427
OpenAlexW2525032631

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.